chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71504526615045267AACTCTCTCT3GENIChomozygous54956133
71504652815046529TG37GENIChomozygous53799405
71504700815047009AC31GENIChomozygous53799407
71504718815047189GA32GENIChomozygous53799409
71504749315047494CCCCT30GENIChomozygous53799410
71504808115048082AT33GENIChomozygous53799412
71505255015052551TC32GENIChomozygous53799422
71505255815052559TC37GENIChomozygous53799423
71505331915053320AC33GENIChomozygous53799425
71505628715056288GA31GENIChomozygous53799426
71505730315057304C-22GENIChomozygous53799428
71505760115057602GGAACA30GENIChomozygous53799429
71505800515058006TC29GENIChomozygous53799431
71505825115058252CCT18GENICpossibly homozygous53799433
71505842515058426GGTATAGA24GENIChomozygous53799438
71505882415058825G-23GENIChomozygous53799439
71505889515058896GA33GENIChomozygous53799441
71505966215059663GGA18GENICpossibly homozygous53799443
71506054015060541GA31GENIChomozygous53799445
71506059515060596GA22GENIChomozygous53799447
71506066215060663AT32GENIChomozygous53799449
71506073015060731CT18GENIChomozygous53799450
71506073315060734TC16GENIChomozygous53799452
71506083215060833CT12GENIChomozygous53799454
71506084715060848AG9GENIChomozygous53799455
71506085615060857CG13GENIChomozygous53799457